Gene: C50C3.6
C50C3.6 | Evidence | Person_evidence | WBPerson395 | |||
---|---|---|---|---|---|---|
WBPerson71 | ||||||
SMap | S_parent | Sequence | C50C3 | |||
Chromosome | III | |||||
Identity (5) | ||||||
Gene_info | Gene_class | prp | ||||
GO_term | GO:0003913 | IEA | Inferred_automatically | |||
GO:0006281 | IEA | Inferred_automatically | ||||
Structured_description | Provisional_description | prp-8 is orthologous to the human gene SIMILAR TO U5 SNRNP-SPECIFIC PROTEIN (220 KD), ORTHOLOG OF S. | Person_evidence | WBPerson567 | ||
Curator_confirmed | WBPerson567 | |||||
CEREVISIAE PRP8P (PRPF8; OMIM:607300), which when mutated leads to retinitis pigmentosa-13 (OMIM:600059). | ||||||
Concise_description | prp-8 is orthologous to the human gene SIMILAR TO U5 SNRNP-SPECIFIC PROTEIN (220 KD), ORTHOLOG OF S. | |||||
Molecular_info (5) | ||||||
Experimental_info | RNAi_result | JA:C50C3.6 | ||||
Simmer:C50C3.6 | ||||||
TH:302H10 | ||||||
Cenix:302-h10 | ||||||
WB_RNAi_result | TH:302H10 | |||||
JA:C50C3.6 | ||||||
Simmer:C50C3.6 | ||||||
Cenix:302-h10 | ||||||
Expr_pattern | Expr5928 | |||||
Y2H_target (2) | ||||||
Reference | WBPaper00026080 | |||||
Method | Gene |